2 ML sibeprenlimab-szsi 200 MG/ML Prefilled Syringe — RxCUI 2728400
RxNorm drug concept · Semantic clinical drug
RxCUI 2728400
Semantic clinical drug · SCD
● Current RxNorm concept 1 FDA product
1 package NDC
Snapshot Jul 14, 2026
What you’re looking at: the standardized identity of one medicine, as the U.S. drug-data system sees it. Below — every FDA-listed product, package code, price benchmark, and billing code that maps to it.
🗂️ Key Facts
RxCUI2728400
Official name2 ML sibeprenlimab-szsi 200 MG/ML Prefilled Syringe
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known assibeprenlimab-szsi 400 MG per 2 ML Prefilled Syringe; sibeprenlimab-szsi 400 MG in 2 ML Prefilled Syringe
FDA products mapped1
Package NDCs mapped1
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
🕸️ Concept Web — How 2 ML sibeprenlimab-szsi 200 MG/ML Prefilled Syri... Connects
One RxCUI never lives alone. Follow the path from the raw ingredient down to the exact strength-and-form concepts FDA products carry — every stop is a real RxNorm concept with its own identifier. Hover or focus any chip for what it means.
This page's concept
2 ML sibeprenlimab-szsi 200 MG/ML Prefilled Syringe
RxCUI 2728400 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
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Ingredients 2
The active substance itself — no strength, form, or brand attached yet.
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Sibeprenlimab
2728380IN -
Sibeprenlimab-szsi
2728394PIN
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Sibeprenlimab
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Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
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Voyxact
2728402BN
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Voyxact
-
Dose forms 9
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
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Sibeprenlimab Prefilled Syringe
2728397SCDF -
Sibeprenlimab-szsi Prefilled Syringe
2728399SCDFP -
Sibeprenlimab Injectable Product
2728396SCDG -
Sibeprenlimab-szsi Injectable Product
2728398SCDGP -
Sibeprenlimab Prefilled Syringe [Voyxact]
2728405SBDF -
Sibeprenlimab-szsi Prefilled Syringe [Voyxact]
2728406SBDFP -
Voyxact Injectable Product
2728404SBDG -
Prefilled Syringe
721656DF - +1 more in this family
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Sibeprenlimab Prefilled Syringe
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Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
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Sibeprenlimab-szsi 200 MG/ML
2728395SCDC -
2 ML sibeprenlimab-szsi 200 MG/ML Prefilled Syringe [Voyxact]
2728407SBD -
Sibeprenlimab-szsi 200 MG/ML [Voyxact]
2728403SBDC
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Sibeprenlimab-szsi 200 MG/ML
Showing up to 8 concepts per family — 14 of 15 stored related concepts drawn.
These are official RxNorm vocabulary relationships — how concepts name and organize the same medicine. They do not establish therapeutic equivalence or substitutability: two concepts appearing in one web is never a statement that products can be swapped.
🔀 Generic ⇄ Brand Crosswalk
The same medicine has an unbranded (generic) identity and one or more brand-name identities — each with its own RxCUI. This is a naming relationship in RxNorm, not a statement that any two products are substitutable.
Generic (Clinical) Concepts
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Sibeprenlimab-szsi 200 MG/ML
SCDC · 2728395 -
Sibeprenlimab Prefilled Syringe
SCDF · 2728397 -
Sibeprenlimab-szsi Prefilled Syringe
SCDFP · 2728399 -
Sibeprenlimab Injectable Product
SCDG · 2728396 -
Sibeprenlimab-szsi Injectable Product
SCDGP · 2728398
Brand-Name Concepts
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2 ML sibeprenlimab-szsi 200 MG/ML Prefilled Syringe [Voyxact]
SBD · 2728407 -
Sibeprenlimab-szsi 200 MG/ML [Voyxact]
SBDC · 2728403 -
Sibeprenlimab Prefilled Syringe [Voyxact]
SBDF · 2728405 -
Sibeprenlimab-szsi Prefilled Syringe [Voyxact]
SBDFP · 2728406 -
Voyxact Injectable Product
SBDG · 2728404 -
Voyxact
BN · 2728402
📦 FDA Products & Package NDCs
1 product · 1 package NDC
1 package NDC map to RxCUI 2728400 in the current snapshot — up to 50 per page. Each linked NDC opens its full package page.
| Package NDC | Package | Brand / generic name | Labeler | Marketing start |
|---|---|---|---|---|
| 59148-0400-75 | 1 SYRINGE in 1 CARTON (59148-400-75) / 2 mL in 1 SYRINGE | VOYXACT | Otsuka America Pharmaceutical, Inc. | 2025-11-25 |
Observed labelers:
Otsuka America Pharmaceutical, Inc. (1)
— this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.
🗃️ Sources & Limits
Atlas generation902fddb9-e9c1-4004-bf4c-dba4d51037c7
openFDA export observedJul 14, 2026
RxNorm release07/06/2026
Methodology2026-07-full-catalog-v1
- A shared RxCUI does not prove interchangeability. Products mapped to the same concept are not thereby equivalent or substitutable — equivalence is a separate, product-level determination.
- Listing here does not establish approval or coverage. Appearing in this snapshot is a data observation, not an FDA approval status or a payer coverage decision.
- Missing data never means zero. A silent dataset (no price, no billing code, no utilization) means no observation — not that the real-world value is zero.
- Counts describe the mapping footprint. Product, package, and labeler counts are the FDA-listed mapping footprint in this snapshot — not sales, inventory, availability, or market share.
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.
Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.